Skip to content

Nutritional Intervention before liver transpantation (LTx)

Nutritional Intervention before liver transpantation (LTx)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00023353
Enrollment
125
Registered
2020-11-09
Start date
2020-11-09
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Z75.67

Interventions

Group 1: standardized questionnaire regarding nutritional status (PG-SGA) / NRS score / 6 min. Walking test / hand strength / BIA measurement for new listings for liver transplantation and after 12 we

Sponsors

Medizinische Klinik und Poliklinik IIKlinikum der Universität München
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: listed to liver transplantation on the basis of liver cirrhosis / oral or enteral nutrition / adults / the written informed consent

Exclusion criteria

Exclusion criteria: Intolerance to oral supplements / only parenteral nutrition possible / patients with a pacemaker (KI for BIA measurement) / minor patients / people who are temporarily or permanently unable to give their consent / pregnant patients / patients requiring intensive care

Design outcomes

Primary

MeasureTime frame
Increase in the phase angle in the bioelectrical impedance measurement (BIA measurement) by 20% after 12 weeks

Secondary

MeasureTime frame
- Increase in hand strength - Improvement of the 6 min walking test - Biochemical parameters (albumin, total protein) - Less frequent hospital stays during the waiting period and shorter hospitilation during transplantation - Improvement in quality of life and nutritional status (PG-SGA score) - Measurement of the skeletal muscle index in the context of radiological tomography to assess sarcopenia over the course - lower mortality

Countries

Germany

Contacts

Public ContactAstrid Konrad-Zerna

Medizinische Klinik und Poliklinik IIKlinikum der Universität München

Astrid.Konrad@med.uni-muenchen.de08944000

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026